Quality Control Chemist

Job ID 17-00191

Industry Pharma

Job Type Permanent

Location Somerset, NJ


This position is primarily responsible for testing samples using a wide range of analytical methodology. Reviewing, preparation/maintenance of SOPs and STP's, calibration and other controlled document, to ensure quality of the dietary Supplement by performing the following duties.

- Personal responsibility for following safety rules, SOPs and cGMPs guidelines.
- To prepare and conduct all chemical testing and various analytical testing procedures. on samples from all phases (Raw material, Finished Product, In-Process and Packaged product) according to Standard testing procedure (STP).
- Responsible to prepare accurate daily records and documents that report the results of their lab work.
- Adapt, maintain and operate analytical instrumentation such as HPLC, GC, FTIR, TOC, UV, etc. and minor trouble shooting of equipment.
- Documentation of log books, in-house calibration records, temperature and humidity records, etc.
- Perform safety and housekeeping aspects of the job by following all safety rules, wearing required safety equipment, keeping work areas clean during and at completion of tasks, maintaining all work stations and equipment in an orderly and clean fashion.
- Maintain monthly inventory on supplies for QC for devices and reagents and standards.
- Ensures that all paperwork is properly documented.
- Keeps accurate attendance records; files proper reports (accident, probation, etc.).
- Will assist in QC stability testing, prepare and maintain stability records and summaries.
- Responsible for the preparation and review of Standard operating procedure or Standard testing procedure.
- Performs other duties as and when assigned.


At least a bachelor's degree or master degree in the field; minimum 3-5 years related experience and/or training; or equivalent combination of education and experience.